Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Qiang-Wei Liu"'
Autor:
Long Feng, Zhi‐Gao Sun, Qiang‐wei Liu, Tao Ma, Zhi‐Peng Xu, Ze‐Guo Feng, Wei‐xiu Yuan, Hong Zhang, Long‐he Xu
Publikováno v:
Brain and Behavior, Vol 10, Iss 11, Pp n/a-n/a (2020)
Abstract Objective Propofol is one of the most commonly used intravenous drugs to induce and maintain general anesthesia. In vivo and in vitro studies have shown that propofol can affect neuronal growth, leading to apoptosis and impairing cognitive f
Externí odkaz:
https://doaj.org/article/b9a24a9f91dc46568d22339912751f53
Publikováno v:
Frontiers in Oncology, Vol 9 (2019)
Background and Objectives: Our aim was to investigate whether the modified American Joint Committee on Cancer (AJCC) tumor-node-metastasis (TNM) staging system based on the node ratio can further improve the capacity of prognosis assessment for gastr
Externí odkaz:
https://doaj.org/article/6bdfc67edc9c4c67a9c6b50a62d3af4a
Publikováno v:
Frontiers in Pain Research. 2
Background: Bone cancer pain (BCP) significantly affects patient quality of life, results in great bodily and emotional pain, and creates difficulties in follow-up treatment and normal life. Transient receptor potential ankyrin 1 (TRPA1) is an essent
Autor:
Zhi-Gao Sun, Zhipeng Xu, Longhe Xu, Tao Ma, Ze-Guo Feng, Qiang‐wei Liu, Hong Zhang, Weixiu Yuan, Long Feng
Publikováno v:
Brain and Behavior, Vol 10, Iss 11, Pp n/a-n/a (2020)
Brain and Behavior
Brain and Behavior
Objective Propofol is one of the most commonly used intravenous drugs to induce and maintain general anesthesia. In vivo and in vitro studies have shown that propofol can affect neuronal growth, leading to apoptosis and impairing cognitive function.
Publikováno v:
Organic Letters. 15:3974-3977
A new β-stereoselective D- and L-arabinofuranosylation method has been developed employing 5-O-(2-quinolinecarbonyl) substituted arabinosyl ethyl thioglycosides as glycosyl donors. The approach allows a wide range of acceptor substrates to be used;
Publikováno v:
Organic & Biomolecular Chemistry. 11:3903
We describe in this paper the efficient four-component one-pot synthesis of three fully protected oligosaccharides 22, 36, and 50 with di-branched structures by employing D-galacto- and mannopyranosyl thioglycoside diols as central glycosylating agen